A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057729



Internal ID20624769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21304045..21308131hg38UCSC Ensembl
chr1:21630538..21634624hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg384087
hg194087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321916
Supporting Variants
Samples
Known GenesECE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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